T6SS-associated Rhs toxin containers: Structural and functional insights into bacterial weaponry and self-protection

No abstract is available for this paper.

• Publication year

  2024

• Venue

  bioRxiv

• Publication date

  2024-02-27

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1101/2024.02.26.582050
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Structure of a bacterial Rhs effector exported by the type VI secretion system

  2021influential reference
• Mounting, structure and autocleavage of a type VI secretion-associated Rhs polymorphic toxin

  2021influential reference
• An antibacterial T6SS in Pantoea agglomerans pv. betae delivers a lysozyme‐like effector to antagonize competitors

  2021cited by this paper
• Highly accurate protein structure prediction with AlphaFold

  2021influential reference
• Identification of type VI secretion system toxic effectors using adaptors as markers

  2020cited by this paper
• Intramolecular chaperone-mediated secretion of an Rhs effector toxin by a type VI secretion system

  2020influential reference
• Polymorphic Toxins and Their Immunity Proteins: Diversity, Evolution, and Mechanisms of Delivery.

  2020cited by this paper
• Bioinformatic Analysis of the Type VI Secretion System and Its Potential Toxins in the Acinetobacter Genus

  2019cited by this paper
• CDD/SPARCLE: the conserved domain database in 2020

  2019cited by this paper
• The Type VI secretion system: a versatile bacterial weapon.

  2019cited by this paper
• Tc toxin activation requires unfolding and refolding of a β-propeller

  2018influential reference
• A type VI secretion system effector delivery mechanism dependent on PAAR and a chaperone–co-chaperone complex

  2018cited by this paper
• CASTp 3.0: computed atlas of surface topography of proteins

  2018influential reference
• Mechanism of loading and translocation of type VI secretion system effector Tse6

  2018cited by this paper
• Type VI Secretion Effectors: Methodologies and Biology

  2017cited by this paper
• The CDI toxin of Yersinia kristensenii is a novel bacterial member of the RNase A superfamily

  2017influential reference
• Improvements to the APBS biomolecular solvation software suite

  2017cited by this paper
• In vivo structures of an intact type VI secretion system revealed by electron cryotomography

  2017cited by this paper
• PAAR‐Rhs proteins harbor various C‐terminal toxins to diversify the antibacterial pathways of type VI secretion systems

  2017cited by this paper
• Bacterial Secretion Systems: An Overview

  2016cited by this paper
• SeqKit: A Cross-Platform and Ultrafast Toolkit for FASTA/Q File Manipulation

  2016cited by this paper
• Structure of the T4 baseplate and its function in triggering sheath contraction

  2016cited by this paper
• Intraspecies Competition in Serratia marcescens Is Mediated by Type VI-Secreted Rhs Effectors and a Conserved Effector-Associated Accessory Protein

  2015cited by this paper
• Identification of divergent type VI secretion effectors using a conserved chaperone domain

  2015cited by this paper
• SecReT6: a web-based resource for type VI secretion systems found in bacteria.

  2015cited by this paper
• An interbacterial NAD(P)(+) glycohydrolase toxin requires elongation factor Tu for delivery to target cells.

  2015cited by this paper
• Molecular weaponry: diverse effectors delivered by the Type VI secretion system

  2015cited by this paper
• Mechanism of Tc toxin action revealed in molecular detail

  2014influential reference
• VgrG, Tae, Tle, and beyond: the versatile arsenal of Type VI secretion effectors.

  2014cited by this paper
• Rhs proteins from diverse bacteria mediate intercellular competition

  2013cited by this paper
• The BC component of ABC toxins is an RHS-repeat-containing protein encapsulation device

  2013influential reference
• PAAR-repeat proteins sharpen and diversify the Type VI secretion system spike

  2013influential reference
• Polymorphic toxin systems: Comprehensive characterization of trafficking modes, processing, mechanisms of action, immunity and ecology using comparative genomics

  2012cited by this paper
• Type VI secretion requires a dynamic contractile phage tail-like structure

  2012cited by this paper
• Comparative genomics of the type VI secretion systems of Pantoea and Erwinia species reveals the presence of putative effector islands that may be translocated by the VgrG and Hcp proteins

  2011cited by this paper
• CDD: a Conserved Domain Database for the functional annotation of proteins

  2010cited by this paper
• Rational Design of a Plasmid Origin That Replicates Efficiently in Both Gram-Positive and Gram-Negative Bacteria

  2010cited by this paper
• A type VI secretion system of Pseudomonas aeruginosa targets a toxin to bacteria.

  2010cited by this paper
• Data Structures for Statistical Computing in Python

  2010influential reference
• Remodelling of VipA/VipB tubules by ClpV‐mediated threading is crucial for type VI protein secretion

  2009cited by this paper
• Evolutionary diversification of an ancient gene family (rhs) through C-terminal displacement

  2009cited by this paper
• Type VI secretion apparatus and phage tail-associated protein complexes share a common evolutionary origin

  2009cited by this paper
• Biopython: freely available Python tools for computational molecular biology and bioinformatics

  2009cited by this paper
• Type VI secretion system translocates a phage tail spike-like protein into target cells where it cross-links actin

  2007cited by this paper
• The relationships between the isoelectric point and: length of proteins, taxonomy and ecology of organisms

  2007cited by this paper
• Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system

  2006cited by this paper
• Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes.

  2001influential reference

• No citing papers are available for this paper.